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Diabetic Neuropathies clinical trials

View clinical trials related to Diabetic Neuropathies.

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NCT ID: NCT00150423 Completed - Clinical trials for Diabetic Neuropathy, Painful

To Evaluate the Safety and Efficacy of Pregabalin in Patients With Painful Diabetic Peripheral Neuropathy.

Start date: January 2001
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of pregabalin in patients with painful diabetic peripheral neuropathy.

NCT ID: NCT00143156 Completed - Clinical trials for Diabetic Neuropathies

Pregabalin vs Placebo in Treatment of Neuropathic Pain Associated With Diabetic Peripheral Neuropathy

Start date: March 2005
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of pregabalin administered twice a day compared to placebo in reducing pain in subjects with painful diabetic peripheral neuropathy.

NCT ID: NCT00141401 Completed - Clinical trials for Diabetic Neuropathy, Painful

Safety and Efficacy of Pregabalin in Patients With Diabetic Peripheral Neuropathy.

Start date: September 1999
Phase: Phase 3
Study type: Interventional

To evaluate long-term efficacy and safety of pregabalin in patients with diabetic peripheral neuropathy.

NCT ID: NCT00141219 Completed - Clinical trials for Diabetic Neuropathies

Pregabalin Peripheral Neuropathic Pain Study

Start date: December 2005
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of pregabalin, using a flexible, optimized dose schedule with dose adjustment based on Daily Pain Rating Scale (DPRS), compared to placebo in subjects with peripheral neuropathic pain.

NCT ID: NCT00135109 Completed - Clinical trials for Diabetic Neuropathies

Trial to Assess the Efficacy and Safety of SPM 927 (200, 400, and 600mg/Day) in Subjects With Painful Distal Diabetic Neuropathy

Start date: October 2004
Phase: Phase 3
Study type: Interventional

This phase 3 trial is being conducted at approximately 80 sites in the United States (U.S.) to investigate whether lacosamide (SPM 927) at different doses reduces pain in subjects with diabetic neuropathy. Approximately 455 subjects will be randomized to placebo or to one of three doses of lacosamide. To qualify for this trial, subjects with symptoms of painful distal diabetic neuropathy ranging in duration from 6 months to 5 years must have an average pain intensity of greater than or equal to 4 on an 11-point Likert scale (0-10 scale) during the 7 day period prior to the start of treatment. To determine what effect lacosamide has on diabetic neuropathic pain, subjects will use a diary to record their daily pain intensity (morning and evening; and pain interference with sleep (morning) and activity (evening). Use of rescue medication (acetaminophen) and subjects' quality of life will be investigated. In addition, the safety and tolerability of the different doses of lacosamide will be investigated.

NCT ID: NCT00120341 Completed - Diabetes Mellitus Clinical Trials

Anodyne Therapy in Diabetic Sensory Neuropathy

Start date: April 2005
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to determine if the use of a series of the Anodyne Therapy System in-home treatments over a 90-day period will improve peripheral sensation and quality of life in persons with diabetes mellitus.

NCT ID: NCT00116207 Completed - Clinical trials for Diabetic Autonomic Neuropathy

An Intervention Trial for Cardiac Neuropathy in Type 1 Diabetes

Start date: January 2000
Phase: Phase 3
Study type: Interventional

The focus of this project is cardiovascular diabetic autonomic neuropathy (DAN). DAN affects the nerves that control heart rate and blood flow to the heart in people with diabetes. DAN may cause problems with the rhythm of the heartbeat or decrease blood flow to the heart. Three medications will be tested for their effectiveness in DAN.

NCT ID: NCT00113620 Completed - Pain Clinical Trials

Safety and Efficacy of Dextromethorphan and Quinidine in the Treatment of the Pain of Diabetic Neuropathy

Start date: July 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether dextromethorphan (Neurodex) and quinidine are effective in the treatment of pain of diabetic neuropathy.

NCT ID: NCT00110500 Completed - Diabetic Neuropathy Clinical Trials

Clinical Trial of SB-509-0401 in Subjects With Diabetic Neuropathy

Start date: April 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the clinical and laboratory safety of SB-509 when given as a single treatment by an intramuscular injection to subjects with diabetic neuropathy.

NCT ID: NCT00105755 Completed - Diabetes Mellitus Clinical Trials

Dermal Thermometry and Self-Care of High Risk Diabetic Patients

Start date: January 2003
Phase: N/A
Study type: Interventional

Foot ulcers remain the most common reason for hospital admission among veterans with diabetes. Healing and preventing these wounds should be a high priority for clinicians treating these high-risk patients. Previous work by the investigators has suggested that diabetic foot ulcers are preceded by inflammation, which can potentially be detected with a thermometer.